Transcription of Deviation Handling and Quality Risk Management
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Deviation Handling and Quality Risk Management
Deviation Handling and Quality Risk Management A note for guidance for the manufacture of prequalified vaccines for supply to United Nations agencies July, 2013 Vaccine Quality and Regulations (VQR), Essential Medicines and Health Products World Health Organization (WHO), Geneva, Switzerland Deviation Handling and Quality Risk Management 2 This guidance document Deviation Handling and Quality Risk Management is one of a series developed by WHO/EMP/HIS Quality , Safety & Standards team upon request from the manufacturers members of the Developing Countries Vaccine Manufacturers Network (DCVMN), with funds of USAID. A set of priority topics has been identified by vaccine manufacturers for WHO to provide guidance on expectations from the vaccine prequalification programme. The guidance document is targeted at manufacturers who are new to the prequalification of vaccines or who require guidance on the level of detail needed for risk assessment for Deviation Management activities.
recorded in batch record or logbook, as appropriate) in case it needs to be retrieved later as part of an investigation as applicable. The following are possible examples of incidents. It is noted that each event needs to be analyzed as described above developing an objective and justified criteria avoiding the natural bias from
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